Evidence map›Paper›PMID 24694239›Full record

ArticleBMC genomics2014

Genome-wide variations in a natural isolate of the nematode Caenorhabditis elegans.

Ismael A Vergara, Maja Tarailo-Graovac, Christian Frech, Jun Wang, Zhaozhao Qin, Ting Zhang, Rong She, Jeffrey S C Chu, Ke Wang, Nansheng Chen

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.3field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 54 citations in OpenAlex.

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  8. All the microbiology nematodes can teach us.FEMS microbiology ecology · 2016
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Ismael A Vergara
Maja Tarailo-Graovac
Christian Frech
Jun Wang
Zhaozhao Qin
Ting Zhang
Rong She
Jeffrey S C Chu
Ke Wang
Nansheng ChenDepartment of Molecular Biology and Biochemistry, Simon Fraser University, 8888 University Drive, Burnaby, British Columbia V5A 1S6, Canada. chenn@sfu.ca.
Simon Fraser University · CA

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

backgroundIncreasing genetic and phenotypic differences found among natural isolates of C. elegans have encouraged researchers to explore the natural variation of this nematode species.

resultsHere we report on the identification of genomic differences between the reference strain N2 and the Hawaiian strain CB4856, one of the most genetically distant strains from N2. To identify both small- and large-scale genomic variations (GVs), we have sequenced the CB4856 genome using both Roche 454 (~400 bps single reads) and Illumina GA DNA sequencing methods (101 bps paired-end reads). Compared to previously described variants (available in WormBase), our effort uncovered twice as many single nucleotide variants (SNVs) and increased the number of small InDels almost 20-fold. Moreover, we identified and validated large insertions, most of which range from 150 bps to 1.2 kb in length in the CB4856 strain. Identified GVs had a widespread impact on protein-coding sequences, including 585 single-copy genes that have associated severe phenotypes of reduced viability in RNAi and genetics studies. Sixty of these genes are homologs of human genes associated with diseases. Furthermore, our work confirms previously identified GVs associated with differences in behavioural and biological traits between the N2 and CB4856 strains.

conclusionsThe identified GVs provide a rich resource for future studies that aim to explain the genetic basis for other trait differences between the N2 and CB4856 strains.

Indexed as

Genetic VariationGenome, HelminthAnimalsBase CompositionCaenorhabditis elegansChromosome MappingCodonComparative Genomic HybridizationComputational BiologyDNA Transposable ElementsDrug ResistanceGenetic Association StudiesGenotypeHigh-Throughput Nucleotide SequencingINDEL MutationMultigene FamilyCodonDNA Transposable Elements

Identifiers

PMID24694239
PMCPMC4023591
OpenAlexW2147852901

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.